A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057092



Internal ID19146311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32369618..33807304hg38UCSC Ensembl
Innerchr16:32380939..33609771hg19UCSC Ensembl
Innerchr16:32288440..33517272hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381437687
hg191228833
hg181228833
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2871n100
Supporting Variantsnssv3551092, nssv3551093
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057092
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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